It is great that your daughter is very accepting. It is so important that she never sees herself or feels different from her friends. You may want to contact the Chidrens Alopecia Project and get on their list. They maybe able to help you locate a family in your area. In Aug they will have Alopeciapalooza and weekend at a camp for the kids and their families. www.childrensalopeciaproject.org. take care,Cindy
Hi Lauren, welcome to AW. Are you doing? I have an 8 yr old daughter with this condition who has handled it all so exceptionally well. If you haven't I suggest contacting the Children's Alopecia Project. They can offer some great supports and maybe help you connect with a family in your area. Cindy
Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.
Comment Wall (2 comments)
You need to be a member of Alopecia World to add comments!
Join Alopecia World